| Diseases |
Alias |
|
| Spinocerebellar Ataxia 1 |
|
Spinocerebellar Ataxia Type 1
|
SCA1
|
|
Olivopontocerebellar Atrophy I
|
Opca1
|
|
Opca4
|
Menzel Type Opca
|
|
Schut-Haymaker Type Opca
|
Spinocerebellar Atrophy I
|
|
Opca I
|
Olivopontocerebellar Atrophy Iv
|
|
Opca Iv
|
Cerebelloparenchymal Disorder I
|
|
Cpd1
|
Olivopontocerebellar Atrophy 1
|
|
Cerebelloparenchymal Disorder 1
|
Olivopontocerebellar Atrophy 4
|
|
Spinocerebellar Atrophy 1
|
Type 1 Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxia-1
|
Ataxia, Spinocerebellar, Type 1
|
|
|
| Primary Cerebellar Degeneration |
|
Spinocerebellar Degenerations
|
Cerebellar Degenerations, Primary
|
|
Spinocerebellar Degeneration
|
|
|
| Hereditary Ataxia |
|
Sca
|
Spinocerebellar Ataxia
|
|
Ataxias Hereditary
|
Ataxias, Hereditary
|
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
Spinocerebellar Ataxia
|
Adca
|
|
Pierre Marie Cerebellar Ataxia
|
Ataxia, Spinocerebellar
|
|
Sca
|
Autosomal Dominant Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxias
|
|
|
| Spinocerebellar Ataxia 12 |
|
Spinocerebellar Ataxia Type 12
|
SCA12
|
|
Ataxia, Spinocerebellar, Type 12
|
|
|
| Dentatorubral-Pallidoluysian Atrophy |
|
DRPLA
|
Naito-Oyanagi Disease
|
|
Haw River Syndrome
|
Myoclonic Epilepsy With Choreoathetosis
|
|
Nod
|
Ataxia, Chorea, Seizures, And Dementia
|
|
Dentatorubropallidoluysian Atrophy
|
Hrs
|
|
Naito Oyanagi Disease
|
Dentatorubral Pallidoluysian Atrophy
|
|
Dentatorubro-Pallidoluysian Atrophy
|
Myoclonic Epilepsies, Progressive
|
|
Atrophy, Pallidoluysian, Dentatorubral
|
|
|
| Machado-Joseph Disease |
|
SCA3
|
MJD
|
|
Spinocerebellar Ataxia 3
|
Azorean Disease
|
|
Spinocerebellar Ataxia Type 3
|
Spinocerebellar Atrophy
|
|
Azorean Neurologic Disease
|
Spinopontine Atrophy
|
|
Nigrospinodentatal Degeneration
|
Spinocerebellar Atrophy Iii
|
|
Spinocerebellar Atrophy Type 3
|
Azorean Ataxia
|
|
Azorean Disease Of The Nervous System
|
Machado Disease
|
|
Nigro-Spino-Dentatal Degeneration With Nuclear Ophthalmoplegia
|
Disease, Machado-Joseph
|
|
Ataxia, Spinocerebellar
|
|
|
| Spinocerebellar Ataxia 17 |
|
Spinocerebellar Ataxia Type 17
|
SCA17
|
|
Huntington Disease-Like 4
|
Hdl4
|
|
Olivopontocerebellar Atrophy V
|
Cerebelloparenchymal Disorder Ii
|
|
Opca5
|
Cpd2
|
|
Sca 17
|
Ataxia, Spinocerebellar, Type 17
|
|
|
| Friedreich Ataxia |
|
Friedreich Ataxia 1
|
FRDA
|
|
Friedreich Ataxia With Retained Reflexes
|
Frda1
|
|
Fa
|
Friedreich'S Ataxia
|
|
Hereditary Spinal Ataxia
|
Fa1
|
|
Friedreich'S Tabes
|
Hereditary Spinal Sclerosis
|
|
Spinocerebellar Ataxia, Friedreich
|
Friedreich Spinocerebellar Ataxia
|
|
Friedrich'S Ataxia
|
|
|
| Multiple System Atrophy 1 |
|
Multiple System Atrophy
|
Shy-Drager Syndrome
|
|
Msa
|
MSA1
|
|
Multiple System Atrophy 1, Susceptibility To
|
Sporadic Olivopontocerebellar Atrophy
|
|
Multisystem Atrophy
|
Msa1, Susceptibility To
|
|
Multiple System Atrophy, Susceptibility To
|
Opca
|
|
Progressive Autonomic Failure With Multiple System Atrophy
|
Sds
|
|
|
| Parkinson Disease 7, Autosomal Recessive Early-Onset |
|
Autosomal Recessive Early-Onset Parkinson Disease 7
|
PARK7
|
|
Parkinson'S Disease 7
|
Autosomal Recessive Early-Onset Parkinson'S Disease 7
|
|
Parkinson Disease 7
|
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex Type 2
|
|
Autosomal Recessive Early-Onset Parkinson Disease Type 7
|
Parkinson Disease, Type 7
|
|
|
| Spinal And Bulbar Muscular Atrophy, X-Linked 1 |
|
Kennedy Disease
|
Sbma
|
|
Spinal And Bulbar Muscular Atrophy
|
Kennedy'S Disease
|
|
X-Linked Spinal And Bulbar Muscular Atrophy
|
SMAX1
|
|
Kd
|
Kennedy Spinal And Bulbar Muscular Atrophy
|
|
Spinobulbar Muscular Atrophy
|
Bulbospinal Muscular Atrophy, X-Linked
|
|
Bulbospinal Neuronopathy, X-Linked Recessive
|
Xbsn
|
|
Spinal And Bulbar Muscular Atrophy Of Kennedy
|
Bulbospinal Muscular Atrophy
|
|
X-Linked Bulbospinal Amyotrophy
|
Bulbo-Spinal Atrophy, X-Linked
|
|
Spinal Bulbar Muscular Atrophy
|
X-Linked Bulbo-Spinal Atrophy
|
|
X-Linked Spinal Bulbar Muscular Atrophy
|
X-Linked Bsma
|
|
X-Linked Bulbospinal Muscular Atrophy
|
Spinal And Bulbar Muscular Atrophy X-Linked 1
|
|
Bulbospinal Muscular Atrophy X-Linked
|
Bulbospinal Neuronopathy X-Linked Recessive
|
|
Kennedy Disease)
|
Kennedy Syndrome
|
|
Atrophy, Muscular, Spinal And Bulbar, Kennedy Type
|
Atrophy, Muscular, Spinobulbar
|
|
Bulbospinal Neuronopathy
|
|
|
| Dementia |
|
Dementias
|
Presenile Dementia
|
|
Alzheimer Type Dementia
|
Alzheimer Sclerosis
|
|
Alzheimer Disease Dementia
|
Alzheimer Dementia
|
|
Primary Degenerative Alzheimer Type Dementia
|
End Stage Alzheimer'S Dementia
|
|
Alzheimer'S Type Atypical Dementia
|
Alzheimer Type Presenile Dementia
|
|
Early Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 2
|
|
Dementia In Alzheimer Disease With Early Onset
|
Early Onset Alzheimer Type Dementia, Uncomplicated
|
|
Primary Degenerative Alzheimer Type Dementia, Early Onset
|
Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated
|
|
Alzheimer Disease Dementia With Early Onset
|
Presenile Sclerosis
|
|
Presenile Brain Sclerosis
|
Presenile Alzheimer Brain Sclerosis
|
|
Late Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 1
|
|
Dementia In Alzheimer Disease With Late Onset
|
Primary Degenerative Alzheimer Type Dementia, Late Onset
|
|
Sdat - [Senile Dementia, Alzheimer Type]
|
Alzheimer Disease Dementia With Late Onset
|
|
Late Onset Alzheimer Brain Sclerosis
|
Senile Alzheimer Brain Disease
|
|
Senile Alzheimer Brain Sclerosis
|
Senile Primary Degenerative Alzheimer Type Dementia
|
|
Senile Dementia Of The Alzheimer Type
|
Arteriosclerotic Dementia
|
|
Strategic-Infarct Dementia
|
Post Stroke Dementia
|
|
Vascular Cognitive Impairment
|
Vascular Dementia
|
|
Dementia Of The Lewy Body Type
|
Dementia With Lewy Bodies
|
|
Sdlt - [Senile Dementia Of The Lewy Body Type]
|
Senile Dementia Of The Lewy Body Type
|
|
Alcohol-Related Dementia
|
Alcoholic Dementia Nos
|
|
Alcohol-Induced Dementia
|
Alcoholic Brain Syndrome
|
|
Chronic Alcoholic Brain Syndrome
|
Alcohol Dementia
|
|
Late Onset Alcoholic Psychosis
|
Residual And Late-Onset Alcohol-Induced Psychotic Disorder
|
|
Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder
|
Late-Onset Psychoactive Substance-Induced Psychotic Disorder
|
|
Inhalant Dementia
|
Volatile Solvents Dementia
|
|
Dementia In Paralysis Agitans
|
Pdd - [Parkinson Disease Dementia]
|
|
Dementia Syndrome Of Parkinson Disease
|
Dementia In Parkinson Disease
|
|
Parkinson Related Dementia
|
Dementia In Huntington Chorea
|
|
Hiv - [Human Immunodeficiency Virus] Dementia
|
Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex
|
|
Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex
|
Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex
|
|
Aids Related Dementia
|
Dementia Due To Niacin Deficiency
|
|
|
| Cerebellar Disease |
|
Cerebellar Diseases
|
Cerebellar Dysfunction
|
|
Cerebellar Abnormality
|
Cerebellar Disorders
|
|
|
| Spinocerebellar Ataxia 4 |
|
Spinocerebellar Ataxia Type 4
|
SCA4
|
|
Spinocerebellar Ataxia, Autosomal Dominant, With Sensory Axonal Neuropathy
|
Spinocerebellar Ataxia Autosomal Dominant With Sensory Axonal Neuropathy
|
|
Spinocerebellar Ataxia-4
|
Spinocerebellar Ataxias
|
|
|
| Cerebellar Ataxia Type 47 |
|
|
| Dystonia 12 |
|
DYT12
|
Rdp
|
|
Generalized Dystonia
|
Dystonia-12
|
|
Rapid-Onset Dystonia-Parkinsonism
|
Familial Dystonia
|
|
Dystonia Musculorum Deformans
|
Dystonic Disorders
|
|
Idiopathic Familial Dystonia
|
Dystonia-Parkinsonism, Rapid-Onset
|
|
Fragments Of Torsion Dystonia
|
Dyt-Atp1a3
|
|
Rapid-Onset Dystonia Parkinsonism
|
Rodp
|
|
Dystonia, Type 12
|
Dystonia 3, Torsion, X-Linked
|
|
Idiopathic Non-Familial Dystonia
|
Symptomatic Torsion Dystonia
|
|
Dystonia Disorders
|
|
|
| Spinocerebellar Ataxia 18 |
|
Spinocerebellar Ataxia Type 18
|
SCA18
|
|
Smna
|
Sensorimotor Neuropathy With Ataxia, Autosomal Dominant
|
|
Sensorimotor Neuropathy With Ataxia Autosomal Dominant
|
|
|
| Muscular Atrophy |
|
Muscle Wasting
|
Amyotrophia
|
|
Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
|
| Huntington Disease |
|
Huntington'S Disease
|
Huntington Chorea
|
|
Huntington'S Chorea
|
HD
|
|
Huntington Chronic Progressive Hereditary Chorea
|
Juvenile Huntington Disease
|
|
Chronic Progressive Chorea
|
Chronic Progressive Hereditary Chorea
|
|
Hc - [Huntington Chorea]
|
Hereditary Chorea
|
|
Progressive Hereditary Chorea
|
|
|
| Olivopontocerebellar Atrophy |
|
Thomas Syndrome
|
Olivopontocerebellar Atrophies
|
|
Dejerine-Thomas Syndrome
|
Thomas' Syndrome
|
|
Wadia-Swami Syndrome
|
Opca
|
|
Potter Sequence-Cleft Lip/Palate-Cardiopathy Syndrome
|
Spinocerebellar Ataxia Type 2
|
|
|
| Cerebellar Ataxia Type 48 |
|
|
| Spinocerebellar Ataxia 6 |
|
Spinocerebellar Ataxia Type 6
|
SCA6
|
|
Type 6 Spinocerebellar Ataxia
|
Spinocerebellar Ataxia-6
|
|
Ataxia, Spinocerebellar, Type 6
|
|
|
| Spinocerebellar Ataxia 7 |
|
Spinocerebellar Ataxia Type 7
|
SCA7
|
|
Opca3
|
Opca Iii
|
|
Olivopontocerebellar Atrophy Iii
|
Opca With Retinal Degeneration
|
|
Opca With Macular Degeneration And External Ophthalmoplegia
|
Adca, Type Ii
|
|
Autosomal Dominant Cerebellar Ataxia Type 2
|
Olivopontocerebellar Atrophy 3
|
|
Autosomal Dominant Cerebellar Ataxia, Type Ii
|
Autosomal Dominant Cerebellar Ataxia Type Ii
|
|
Adca2
|
Adcaii
|
|
Ataxia With Pigmentary Retinopathy
|
Cerebellar Syndrome-Pigmentary Maculopathy Syndrome
|
|
Olivopontocerebellar Atrophy With Retinal Degeneration
|
Spinocerebellar Ataxia-7
|
|
Ataxia, Spinocerebellar, Type 7
|
|
|
| Restless Legs Syndrome |
|
Wed
|
Willis-Ekbom Disease
|
|
Restless Leg Syndrome
|
Ekbom Syndrome
|
|
Wittmaack-Ekbom Syndrome
|
Willis Ekbom Disease
|
|
Ekbom'S Syndrome
|
Rls
|
|
Restless Legs
|
Restless Legs Syndrome, Susceptibility To
|
|
|
| Retinal Degeneration |
|
|
| Spinocerebellar Ataxia 14 |
|
Spinocerebellar Ataxia Type 14
|
SCA14
|
|
Ataxia, Spinocerebellar, Type 14
|
|
|
| Dystonia |
|
Dystonic Disease
|
Dystonic Disorder
|
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|
| Episodic Ataxia, Type 2 |
|
Episodic Ataxia Type 2
|
EA2
|
|
Apca
|
Capa
|
|
Cerebellopathy, Hereditary Paroxysmal
|
Acetazolamide-Responsive Hereditary Paroxysmal Cerebellar Ataxia
|
|
Cerebellar Ataxia, Paroxysmal, Acetazolamide-Responsive
|
Episodic Ataxia With Nystagmus
|
|
Ataxia, Episodic, With Nystagmus
|
Episodic Ataxia, Nystagmus-Associated
|
|
Ataxia, Familial Paroxysmal
|
Acetazolamide-Responsive Episodic Ataxia Syndrome
|
|
Acetazolamide-Responsive, Hereditary, Paroxysmal, Cerebellar Ataxia
|
Ataxia, Familial, Paroxysmal
|
|
Nystagmus-Associated Episodic Ataxia
|
Familial Paroxysmal Ataxia
|
|
Episodic Ataxia 2
|
Ea-2
|
|
Episodic Ataxia Nystagmus-Associated
|
Hereditary Paroxysmal Cerebellopathy
|
|
Ataxia, Episodic, Type 2
|
|
|
| Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2 |
|
Aoa2
|
Ataxia With Oculomotor Apraxia Type 2
|
|
Scar1
|
SCAN2
|
|
Ataxia-Oculomotor Apraxia 2
|
Ataxia-Ocular Apraxia 2
|
|
Ataxia-Oculomotor Apraxia Type 2
|
Scan 2
|
|
Spinocerebellar Ataxia With Axonal Neuropathy Type 2
|
Spinocerebellar Ataxia, Autosomal Recessive 1, Formerly
|
|
Scar1, Formerly
|
Autosomal Recessive Spinocerebellar Ataxia-1
|
|
Spinocerebellar Ataxia, Autosomal Recessive, 1
|
Ataxia-Ocular Apraxia-2
|
|
Spinocerebellar Ataxia, Autosomal Recessive 1
|
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2dd |
|
CMT2DD
|
Charcot-Marie-Tooth Neuropathy, Type 2dd
|
|
Charcot-Marie-Tooth Disease Type 2dd
|
Atp1a1-Related Autosomal Dominant Charcot-Marie-Tooth Disease Type 2
|
|
Atp1a1-Related Cmt2
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2dd
|
|
Charcot-Marie-Tooth Disease 2dd
|
|
|
| Gordon Holmes Syndrome |
|
Cerebellar Ataxia And Hypogonadotropic Hypogonadism
|
Lhrh Deficiency And Ataxia
|
|
Cerebellar Ataxia-Hypogonadism Syndrome
|
GDHS
|
|
Cahh
|
Luteinizing Hormone-Releasing Hormone Deficiency With Ataxia
|
|
Gordon-Holmes Syndrome
|
Deficiency Of Luteinizing Hormone-Releasing Hormone With Ataxia
|
|
Luteinizing Hormone-Releasing Hormone, Deficiency Of, With Ataxia
|
Cerebellar Ataxia - Hypogonadism
|
|
Luteinizing Hormone Releasing Hormone, Deficiency Of With Ataxia
|
Ataxia, Cerebellar, And Hypogonadotropic Hypogonadism
|
|
|
| Episodic Ataxia |
|
Isaacs Syndrome
|
Neuromyotonia
|
|
Isaacs' Syndrome
|
Acquired Neuromyotonia
|
|
Continuous Muscle Fiber Activity Syndrome
|
Quantal Squander Syndrome
|
|
Isaacs-Mertens Syndrome
|
Ea Syndrome
|
|
Episodic Ataxia Syndrome
|
Isaac Syndrome
|
|
Isaac'S-Merten'S Syndrome
|
Isaac-Mertens Syndrome
|
|
Peripheral Nerve Hyperexcitability
|
Ea
|
|
Peripheral Nerve Hyperexcitability Syndrome
|
Ataxia, Episodic
|
|
Isaacs Neuromyotonia
|
Continuous Muscle Fibre Activity
|
|
|
| Spinocerebellar Ataxia 8 |
|
Spinocerebellar Ataxia Type 8
|
SCA8
|
|
Ataxia, Spinocerebellar, Type 8
|
|
|
| Autosomal Recessive Cerebellar Ataxia |
|
|
| Choreatic Disease |
|
|
| Spinal Muscular Atrophy |
|
Sma
|
5q Sma
|
|
Proximal Sma
|
Sma-Associated Sma
|
|
Spinal Amyotrophies
|
Spinal Amyotrophy
|
|
Spinal Muscle Degeneration
|
Spinal Muscle Wasting
|
|
Muscular Atrophy Spinal
|
Atrophy, Muscular, Spinal
|
|
Hereditary Motor Neuronopathy
|
Progressive Muscular Atrophy
|
|
Sma - [Spinal Muscular Atrophy]
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Parkinson Disease, Late-Onset |
|
Parkinson Disease
|
Parkinson'S Disease
|
|
PD
|
PARK
|
|
Parkinson Disease, Susceptibility To
|
Late Onset Parkinson'S Disease
|
|
Late Onset Parkinson Disease
|
Paralysis Agitans
|
|
Primary Parkinsonism
|
Idiopathic Parkinson Disease
|
|
Parkinson'S
|
Parkinson Disease, Late-Onset, Susceptibility To
|
|
Parkinson Disease, Age Of Onset, Modifier
|
Lewy Body Parkinson Disease
|
|
Idiopathic Parkinson'S Disease
|
Pd - [Parkinson Disease]
|
|
Parkinson Disease Nos
|
Parkinson, Nos
|
|
Primary Parkinson Disease
|
|
|
| Spastic Ataxia |
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
Amyotrophic Lateral Sclerosis
|
ALS
|
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
|
Charcot Disease
|
ALS1
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
|
Lou Gehrig'S Disease
|
Mnd
|
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
|
Progressive Atrophic Paralysis
|
|
|
| Hereditary Spastic Paraplegia |
|
Familial Spastic Paraplegia
|
Hereditary Spastic Paraparesis
|
|
Strumpell-Lorrain Disease
|
Familial Spastic Paraparesis
|
|
Hsp
|
Spg
|
|
Strümpell-Lorrain Disease
|
Spastic Paraplegia, Hereditary
|
|
French Settlement Disease
|
Strumpell-Lorrain Syndrome
|
|
Fsp
|
Spastic Paraplegia, Familial
|
|
Spastic Paraplegia Hereditary
|
Spastic Paraplegia 3, Autosomal Dominant
|
|
Spastic Paraparesis
|
Hereditary Spastic Paralysis
|
|
Familial Spastic Paralysis
|
Hereditary Spastic Ataxia
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
